Victorch Meditek, Inc. (manufacturer, San Diego, CA): 15 new FDA device listings, incl. applicator, absorbent tipped, sterile

Victorch Meditek, Inc. (San Diego, California): 15 new FDA device listings, incl. applicator, absorbent tipped, sterile. Its amount of 15 is top-decile (96th percentile of 2,570 records). Dated 126 days ago, it serves as a historical benchmark. Score 85/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 15 · 96th percentile of 2,570 DeviceEstablishmentPulse records · 15.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 283 related CA DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentVictorch Meditek, Inc.
Owner / operatorVictorch Meditek Inc
RoleManufacturer
Establishment typesManufacture Device in the United States for Export Only
LocationSan Diego, CA, US
New listings15
DevicesApplicator, Absorbent Tipped, Sterile; Antisera, Fluorescent, Chlamydia Spp.; Wrap, Sterilization; Device, Neurovascular Embolization; Antigen(Complexed),Prostate Specific,(Cpsa); Single (Specified) Analyte Controls (Assayed And Unassayed); Multi-Analyte Respiratory Virus Antigen Detection Test; Test, Luteinizing Hormone (Lh), Over The Counter; Control, Fecal Occult Blood; Scissors, Medical, Disposable
Product codesKXG, LKI, FRG, HCG, NAF, JJX, SCA, NGE, OSL, JOK, LQP, LIP, DDG, LOJ, DJC
Device classesClass I, Class II, Class III
Medical specialtiesGeneral Hospital, Microbiology, Neurology, Clinical Chemistry, Hematology, Immunology, Clinical Toxicology
Brand namesNasopharyngeal Swab; Chlamydia Rapid Test; Hemostatic Patch Bag; HCG pregnancy Urine Rapid Test, HCG Midstream Rapid Test; PSA Rapid Test; CEA Rapid Test; Covid-19/Flu A/Alu B/RSV Rapid Test; LH Rapid test
First new listing2026-06-30
Latest new listing2026-07-02
FDA registration number2032364
Registration expires2026-12-31
amount percentile96th of 2,570 (median 1, 15.0x median)
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL

  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-07-02
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: Victorch Meditek, Inc. and 284 California peers

  • California DeviceEstablishmentPulse records like this one: 284
  • Victorch Meditek, Inc.'s amount: 96th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every California peer: $56,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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85 / 100 Score

  • Brings its own devices to market: buys manufacturing, sterilization and QMS help.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • U.S. establishment.

What is the DeviceEstablishmentPulse record for Victorch Meditek, Inc. in San Diego, California?

Victorch Meditek, Inc. (San Diego, CA), a manufacturer, added 15 FDA device listings between 2026-06-30 and 2026-07-02.

How does Victorch Meditek, Inc. compare to other California DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 15 is 15.0x the median of 1 across 2,570 records. It is 126 days old; check the official source for later updates before acting. Its Score of 85/100 puts it among the stronger signals in this feed.

Victorch Meditek, Inc. vs. top 2 peers

OrganizationLocationAmountPercentileRecord date
Victorch Meditek, Inc.San Diego, CA1596th2026-07-02
Inquis Medical, Inc.Menlo Park, CA587th2026-10-16
Endovascular Engineering, Inc.Menlo Park, CA377th2026-10-14

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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.

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